Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4465ae14a2080673a2d99df3d37e8df6> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B4465ae14a2080673a2d99df3d37e8df6 hasDbXref "NCIT:C97071" @default.
- B4465ae14a2080673a2d99df3d37e8df6 type Axiom @default.
- B4465ae14a2080673a2d99df3d37e8df6 annotatedProperty IAO_0000115 @default.
- B4465ae14a2080673a2d99df3d37e8df6 annotatedSource MONDO_0018840 @default.
- B4465ae14a2080673a2d99df3d37e8df6 annotatedTarget "A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts." @default.